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拟南芥双链RNA结合蛋白DRB3参与甲基化介导的双生病毒防御。

Arabidopsis double-stranded RNA binding protein DRB3 participates in methylation-mediated defense against geminiviruses.

作者信息

Raja Priya, Jackel Jamie N, Li Sizhun, Heard Isaac M, Bisaro David M

机构信息

Department of Molecular Genetics, Center for Applied Plant Sciences, and Center for RNA Biology, The Ohio State University, Columbus, Ohio, USA.

出版信息

J Virol. 2014 Mar;88(5):2611-22. doi: 10.1128/JVI.02305-13. Epub 2013 Dec 18.

Abstract

UNLABELLED

Arabidopsis encodes five double-stranded RNA binding (DRB) proteins. DRB1 and DRB2 are involved in microRNA (miRNA) biogenesis, while DRB4 functions in cytoplasmic posttranscriptional small interfering RNA (siRNA) pathways. DRB3 and DRB5 are not involved in double-stranded RNA (dsRNA) processing but assist in silencing transcripts targeted by DRB2-associated miRNAs. The goal of this study was to determine which, if any, of the DRB proteins might also participate in a nuclear siRNA pathway that leads to geminivirus genome methylation. Here, we demonstrate that DRB3 functions with Dicer-like 3 (DCL3) and Argonaute 4 (AGO4) in methylation-mediated antiviral defense. Plants employ repressive viral genome methylation as an epigenetic defense against geminiviruses, using an RNA-directed DNA methylation (RdDM) pathway similar to that used to suppress endogenous invasive DNAs such as transposons. Chromatin methylation inhibits virus replication and transcription, and methylation-deficient host plants are hypersusceptible to geminivirus infection. Using a panel of drb mutants, we found that drb3 plants uniquely exhibit a similar hypersensitivity and that viral genome methylation is substantially reduced in drb3 compared to wild-type plants. In addition, like dcl3 and ago4 mutants, drb3 plants fail to recover from infection and cannot accomplish the viral genome hypermethylation that is invariably observed in asymptomatic, recovered tissues. Small RNA analysis, bimolecular fluorescence complementation, and coimmunoprecipitation experiments show that DRB3 acts downstream of siRNA biogenesis and suggest that it associates with DCL3 and AGO4 in distinct subnuclear compartments. These studies reveal that in addition to its previously established role in the miRNA pathway, DRB3 also functions in antiviral RdDM.

IMPORTANCE

Plants use RNA-directed DNA methylation (RdDM) as an epigenetic defense against geminiviruses. RNA silencing pathways in Arabidopsis include five double-stranded RNA binding proteins (DRBs) related to Drosophila R2D2 and mammalian TRBP and PACT. While DRB proteins have defined roles in miRNA and cytoplasmic siRNA pathways, a role in nuclear RdDM was elusive. Here, we used the geminivirus system to show that DRB3 is involved in methylation-mediated antiviral defense. Beginning with a panel of Arabidopsis drb mutants, we demonstrated that drb3 plants uniquely show enhanced susceptibility to geminiviruses. Further, like dcl3 and ago4 mutants, drb3 plants fail to hypermethylate the viral genome, a requirement for host recovery. We also show that DRB3 physically interacts with the RdDM pathway components DCL3 and AGO4 in the nucleus. This work highlights the utility of geminiviruses as models for de novo RdDM and places DRB3 protein in this fundamental epigenetic pathway.

摘要

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拟南芥编码五种双链RNA结合(DRB)蛋白。DRB1和DRB2参与微小RNA(miRNA)的生物合成,而DRB4在细胞质转录后小干扰RNA(siRNA)途径中发挥作用。DRB3和DRB5不参与双链RNA(dsRNA)加工,但协助沉默由与DRB2相关的miRNA靶向的转录本。本研究的目的是确定哪些DRB蛋白(如果有的话)可能也参与导致双生病毒基因组甲基化的核siRNA途径。在此,我们证明DRB3与Dicer样3(DCL3)和AGO4蛋白4(AGO4)在甲基化介导的抗病毒防御中发挥作用。植物利用抑制性病毒基因组甲基化作为对抗双生病毒的表观遗传防御机制,使用一种类似于用于抑制内源性侵入性DNA(如转座子)的RNA指导的DNA甲基化(RdDM)途径。染色质甲基化抑制病毒复制和转录,而甲基化缺陷的宿主植物对双生病毒感染高度敏感。使用一组drb突变体,我们发现drb3植物独特地表现出类似的超敏感性,并且与野生型植物相比,drb3中的病毒基因组甲基化显著降低。此外,与dcl3和ago4突变体一样,drb3植物无法从感染中恢复,并且无法完成在无症状的恢复组织中总是观察到的病毒基因组超甲基化。小RNA分析、双分子荧光互补和免疫共沉淀实验表明,DRB3在siRNA生物合成的下游起作用,并表明它在不同的核亚区与DCL3和AGO4结合。这些研究表明,除了其先前在miRNA途径中确定的作用外,DRB3还在抗病毒RdDM中发挥作用。

重要性

植物利用RNA指导的DNA甲基化(RdDM)作为对抗双生病毒的表观遗传防御机制。拟南芥中的RNA沉默途径包括五种与果蝇R2D2以及哺乳动物TRBP和PACT相关的双链RNA结合蛋白(DRB)。虽然DRB蛋白在miRNA和细胞质siRNA途径中有明确的作用,但在核RdDM中的作用却难以捉摸。在此,我们利用双生病毒系统表明DRB3参与甲基化介导的抗病毒防御。从一组拟南芥drb突变体开始,我们证明drb3植物独特地表现出对双生病毒的易感性增强。此外,与dcl3和ago4突变体一样(此处原文有误,推测是想表达“此外,与dcl3和ago4突变体一样”),drb3植物无法使病毒基因组超甲基化,而这是宿主恢复所必需的。我们还表明DRB3在细胞核中与RdDM途径成分DCL3和AGO4发生物理相互作用。这项工作突出了双生病毒作为从头RdDM模型的实用性,并将DRB3蛋白置于这一基本的表观遗传途径中。

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